Linked Data
gnomAD v4:
11-6319506-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319506G>A , CM000673.2:g.6319506G>A | GRCh38 |
| NC_000011.9:g.6340736G>A , CM000673.1:g.6340736G>A | GRCh37 |
| NC_000011.8:g.6297312G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.443C>T MANE Select | ENSP00000307292.3:p.Ala148Val | |
| ENST00000303927.3:c.443C>T | ENSP00000307292.3:p.Ala148Val | |
| ENST00000524852.1:n.229C>T | ||
| ENST00000530979.1:c.539C>T | ENSP00000432047.1:p.Ala180Val | |
| ENST00000532354.1:n.465C>T | ||
| NM_145040.2:c.443C>T | NP_659477.2:p.Ala148Val | |
| XR_930997.1:n.720+1286G>A | ||
| XR_001748106.1:n.117G>A | ||
| XR_242848.4:n.366G>A | ||
| NM_145040.3:c.443C>T MANE Select | NP_659477.2:p.Ala148Val |